Suppr超能文献

德国人群中大量自然流产案例的染色体畸变及文献综述

Chromosome aberrations in a large series of spontaneous miscarriages in the German population and review of the literature.

作者信息

Jenderny Jutta

机构信息

Humangenetik, Labor Lademannbogen, Lademannbogen 61-63, DE-22339 Hamburg, Germany.

出版信息

Mol Cytogenet. 2014 Jun 5;7:38. doi: 10.1186/1755-8166-7-38. eCollection 2014.

Abstract

BACKGROUND

In a review of the literature in 2000 the different cytogenetic aspects of spontaneous miscarriages were well documented. This review also included the spontaneous miscarriage results of one large German study published in 1990. However, to our knowledge there are no new data on spontaneous miscarriages in the German population. Therefore, the aim of the present retrospective large study was to find out the incidence and types of chromosome aberrations in an unselected series of spontaneous miscarriages in the German population, and whether our more recent results were different to data published previously. In case of culture failure we implemented a quantitative fluorescent polymerase chain reaction (QF-PCR) for chromosomes 13, 18, 21, X and Y.

RESULTS

In the present German retrospective study cytogenetic analysis (CA) was attempted on 534 spontaneous miscarriages between weeks 7 and 34 of gestation, being successful in 73% (390/534) of them. Two hundred and thirty-seven of the cases (61%, 237/390) were chromosomally abnormal. Trisomy was the most common chromosome aberration and accounted for 53% (125/237) of the aberrant karyotypes. A multiple aneuploidy was observed in 7% (17/237) of the aberrant karyotypes. Chromosomes 16, 22, 15 and 21 were found most frequently involved in aneuploidies. Fifty-four cases (23%, 54/237) with a polyploidy were found in the present study. Single unbalanced structural chromosome aberrations accounted for 4% (10/237) of the aberrant karyotypes. Eleven samples (5%, 11/237) displayed a variety of numerical and/or structural chromosome aberrations. One hundred and forty-four spontaneous miscarriages (27%, 144/534) failed to grow in culture. A total of 27 cases were analysed by QF-PCR for chromosomes 13, 18, 21, X and Y, being informative in all cases.

CONCLUSION

In our German retrospective large study of spontaneous miscarriages, the incidence and types of chromosome aberrations by CA are within the reported range of other studies published previously before and after 2000. Therefore, we can conclude that cytogenetic aspects of spontaneous miscarriages have not changed over the years. Additionally 8 of 27 cases (30%) without cell growth showed a numerical chromosome aberration by QF-PCR. Therefore QF-PCR played an important role as a supplementary test when culture failure occurred.

摘要

背景

2000年的一篇文献综述对自然流产的不同细胞遗传学方面进行了充分记录。该综述还纳入了1990年发表的一项大型德国研究的自然流产结果。然而,据我们所知,目前尚无关于德国人群自然流产的新数据。因此,本项回顾性大型研究的目的是,在一组未经过筛选的德国人群自然流产病例中,找出染色体畸变的发生率和类型,以及我们最近的结果是否与先前发表的数据有所不同。若培养失败,我们对13、18、21、X和Y染色体实施了定量荧光聚合酶链反应(QF-PCR)。

结果

在本次德国回顾性研究中,对妊娠7至34周的534例自然流产进行了细胞遗传学分析(CA),其中73%(390/534)成功完成分析。其中237例(61%,237/390)存在染色体异常。三体是最常见的染色体畸变类型,占异常核型的53%(125/237)。7%(17/237)的异常核型中观察到多重非整倍体。发现16、22、15和21号染色体最常发生非整倍体改变。本研究中发现54例(23%,54/237)存在多倍体。单一的不平衡结构染色体畸变占异常核型的4%(10/237)。11个样本(5%,11/237)表现出各种数量和/或结构染色体畸变。144例自然流产(27%,144/534)在培养中未生长。共对27例样本进行了13、18、21、X和Y染色体的QF-PCR分析,所有病例均获得有效信息。

结论

在我们对德国自然流产的回顾性大型研究中,通过CA检测到的染色体畸变发生率和类型在2000年前后发表的其他研究报告范围内。因此,我们可以得出结论,多年来自然流产的细胞遗传学特征没有改变。此外,27例无细胞生长病例中有8例(30%)通过QF-PCR检测到数量染色体畸变。因此,当培养失败时,QF-PCR作为一项补充检测发挥了重要作用。

相似文献

4
Incidence and Spectrum of Chromosome Abnormalities in Miscarriage Samples: A Retrospective Study of 330 Cases.
Cytogenet Genome Res. 2019;158(4):171-183. doi: 10.1159/000502304. Epub 2019 Aug 22.
6
Maternal age, history of miscarriage, and embryonic/fetal size are associated with cytogenetic results of spontaneous early miscarriages.
J Assist Reprod Genet. 2019 Apr;36(4):749-757. doi: 10.1007/s10815-019-01415-y. Epub 2019 Feb 9.
7
Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies.
J Obstet Gynaecol Can. 2011 Sep;33(9):955-960. doi: 10.1016/S1701-2163(16)35022-8.

引用本文的文献

3
A case of complex balanced chromosomal translocations associated with adverse pregnancy outcomes.
Mol Cytogenet. 2022 Aug 21;15(1):37. doi: 10.1186/s13039-022-00615-z.
6
Comparative clinical genetic testing in spontaneous miscarriage: Insights from a study in Southern Chinese women.
J Cell Mol Med. 2021 Jun;25(12):5721-5728. doi: 10.1111/jcmm.16588. Epub 2021 May 10.
7
Prenatal diagnosis of sex chromosomal inversion, translocation and deletion.
Mol Med Rep. 2018 Feb;17(2):2811-2816. doi: 10.3892/mmr.2017.8198. Epub 2017 Dec 6.
9
Frequency of Chromosomal Abnormalities in Products of Conception.
Rev Bras Ginecol Obstet. 2017 Mar;39(3):110-114. doi: 10.1055/s-0037-1600521. Epub 2017 Mar 15.

本文引用的文献

2
Second-trimester diagnosis of triploidy: a series of four cases.
AJP Rep. 2013 May;3(1):37-40. doi: 10.1055/s-0032-1331378. Epub 2012 Dec 31.
3
Genetics of early miscarriage.
Biochim Biophys Acta. 2012 Dec;1822(12):1951-9. doi: 10.1016/j.bbadis.2012.07.001. Epub 2012 Jul 13.
5
Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytogenetics.
PLoS One. 2012;7(3):e31282. doi: 10.1371/journal.pone.0031282. Epub 2012 Mar 5.
9
An efficient protocol for the detection of chromosomal abnormalities in spontaneous miscarriages or foetal deaths.
Eur J Obstet Gynecol Reprod Biol. 2009 Dec;147(2):144-50. doi: 10.1016/j.ejogrb.2009.07.023. Epub 2009 Sep 8.
10
Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls.
Genet Med. 2009 Sep;11(9):646-54. doi: 10.1097/GIM.0b013e3181abc92a.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验